Ethylene dimethyl ether

ETHYLENE DIHYDRATE see EJC500 ETHYLENE DIMERCAPTAN see EEBOOO a-ETHYLENE DIMERCAPTAN see EEBOOO ETHYLENE DIMETHYL ETHER see DOE600 ETHYLENE DINITRATE see EJGOOO ETHYLENEDINITRILOTETRAACETIC ACID see EIXOOO... 

ETHYLENE DIMETHYL ETHER (110-71-4) Forms explosive mixture with air (flash point 29°F/—2°C). Violent reaction with strong oxidizers, lithium tetrahydroaluminate. Incompatible with sulfuric acid, isocyanates. May be able to form unstable peroxides upon standing. Flow or agitation of substance may generate electrostatic charges due to low conductivity. 

Ethylene dimethyl ether. See Ethylene glycol dimethyl ether... 

Ethylene dimethyl ether. See Ethylene glycol dimethyl ether Ethylenedinitrilotetraethanol 2,2, 2",2 "-Ethylenedinitrik>tetraethanol. See Tetrahydroxyethyl ethylenediamine... 

Synonyms Dimethoxyethane 1,2-Dimethoxyethane a,p-Dimethoxyethane Dime-thylglycol 2,5-Dioxahexane DME EGDME Ethylene dimethyl ether Glycol dimethyl ether Glyme Monoethylene glycol dimethyl ether Monoglyme... 

Di-alkyl ethers of ethylene glycol, ROCHjCHjOR. The dimethyl ether, b.p. 85°/760 mm., is miscible with water, is a good solvent for organic compounds, and is an excellent inert reaction medium. The diethyl ether (diethyl cdloaolve), b.p. 121-57760 mm., is partially miscible with water (21 per cent, at 20°). 

The chemical recycling of carbon dioxide into usable fuels provides a renewable carbon base to supplement and eventually replace our diminishing natural hydrocarbon resources. Methanol (or dimethyl ether), as discussed, can be readily converted into ethylene or, by further reaction, into propylene. 

Diglyme shown above the arrow in the equation is the solvent in this example Diglyme is an acronym for d/ethylene g/ycol dimethyl ether and its structure is CH3OCH2CH2OCH2CH2OCH3... 

View molecular models of dimethyl ether and ethylene oxide on Learning By Modeling Which one has the greater dipole moment Do the calculated dipole moments bear any relation ship to the observed boiling points (ethylene oxide +10°C dimethyl ether —25°C) d... 

The addition product, C QHgNa, called naphthalenesodium or sodium naphthalene complex, may be regarded as a resonance hybrid. The ether is more than just a solvent that promotes the reaction. StabiUty of the complex depends on the presence of the ether, and sodium can be Hberated by evaporating the ether or by dilution using an indifferent solvent, such as ethyl ether. A number of ether-type solvents are effective in complex preparation, such as methyl ethyl ether, ethylene glycol dimethyl ether, dioxane, and THF. Trimethyl amine also promotes complex formation. This reaction proceeds with all alkah metals. Other aromatic compounds, eg, diphenyl, anthracene, and phenanthrene, also form sodium complexes (16,20). 

Methanol to Ethylene. Methanol to ethylene economics track the economics of methane to ethylene. Methanol to gasoline has been flilly developed and, during this development, specific catalysts to produce ethylene were discovered. The economics of this process have been discussed, and a catalyst (Ni/SAPO 34) with almost 95% selectivity to ethylene has been claimed (99). Methanol is converted to dimethyl ether, which decomposes to ethylene and water the method of preparation of the catalyst rather than the active ingredient of the catalyst has made the significant improvement in yield (100). By optimizing the catalyst and process conditions, it is claimed that yields of ethylene, propylene, or both are maximized. This is still in the bench-scale stage. 

Oxygenates and Chemicals A whole host of oxygenated products, i.e., fuels, fuel additives, and chemicals, can be produced from synthesis gas. These include such produc ts as methanol, ethylene, isobutanol, dimethyl ether, dimethyl carbonate, and many other hydrocarbons and oxyhydrocarbons. Typical oxygenate-producing reactions are ... 

Ethylene glycol dimethyl ether (monoglyme) [110-71-4] M 90.1. See 1,2-dimethoxyethane on... 

Tetrahydrofuran may be purified by refluxing over solid potassium hydroxide, followed by distillation from lithium alu-miniun hydride. Tetrahydrofuran may be replaced by ethylene glycol dimethyl ether (dimethoxyethane). The submitter has indicated that either solvent may be freed conveniently from water, alcohols, and moderate amounts of peroxides by passing the commercial solvent through a column (2 in. diameter X 2-3 ft. length) of Linde Air Products Molecular Sieves (type 13A iQ- n. pellets), at a rate of approximately 100 ml. per minute. 

Aromatic steroids are virtually insoluble in liquid ammonia and a cosolvent must be added to solubilize them or reduction will not occur. Ether, ethylene glycol dimethyl ether, dioxane and tetrahydrofuran have been used and, of these, tetrahydrofuran is the preferred solvent. Although dioxane is often a better solvent for steroids at room temperature, it freezes at 12° and its solvent effectiveness in ammonia is diminished. Tetrahydrofuran is infinitely miscible with liquid ammonia, but the addition of lithium to a 1 1 mixture causes the separation of two liquid phases, one blue and one colorless, together with the separation of a lithium-ammonia bronze phase. Thus tetrahydrofuran and lithium depress the solubilities of each other in ammonia. A tetrahydrofuran-ammonia mixture containing much over 50 % of tetrahydrofuran does not become blue when lithium is added. In general, a 1 1 ratio of ammonia to organic solvents represents a reasonable compromise between maximum solubility of steroid and dissolution of the metal with ionization. 

C) Preparation of 2-Methyl-3-(2,2,2-Trifluoroethyl)Thiomethyl-6-Chloro-7-Sulfamyl-3,4-Dihydro-1,2,4-Benzothiadiazine-1,1-Dioxide To 4.6 g (0.015 mol) of 4-amino-2-chloro-5-(methylsulfamyl)benzenesulfonamide in 30 ml of the dimethyl ether of ethylene glycol is added 4.08 g (0.02 mol) of 2,2,2-trifluoroethylmercaptoacetaldehyde dimethylacetal followed by 1 ml of ethyl acetate saturated with hydrogen chloride gas. The resulting solution is refluxed for 1.5 hours, cooled and then slowly added to cold water dropwise with stirring. The crude product is filtered, dried and recrystallized from isopropanol (3.2 g), MP 202° to 202.5°C. A second recrystallization from isopropanol raised the MP to 202°... 

DME ethylene glycol dimethyl ether TBAI tetra-n-butylammonium iodide... 

The reaction of [CH3Co(salen)H20] with n-C3F7l results in the formation of [ -C3F7Co(salen)] in almost quantitative yield. The reaction occurs in 3 days at room temperature or within 30 minutes on refluxing in ethylene, glycol dimethyl ether 174a). 

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